Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12863738 0.724 0.240 X 136949968 intron variant C/T snv 0.16 14
rs2807264 0.724 0.240 X 136583619 downstream gene variant C/A snv 14
rs17435
MECP2
0.851 0.200 X 154046529 intron variant T/A;C snv 4
rs2294369
CACNA1I
1.000 0.120 22 39679395 missense variant G/A snv 0.23 0.17 1
rs1051266
SLC19A1
0.627 0.640 21 45537880 missense variant T/C;G snv 0.55; 4.4E-06 41
rs2836882 0.724 0.240 21 39094644 intergenic variant G/A snv 0.23 15
rs1127354
ITPA
0.667 0.400 20 3213196 missense variant C/A;G snv 7.5E-02 26
rs2738774 0.724 0.240 20 63637985 downstream gene variant G/A;C snv 14
rs34536443
TYK2
0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 25
rs602662
LOC105447645 ; FUT2
0.716 0.280 19 48703728 missense variant G/A snv 0.40 0.47 16
rs62131887 0.724 0.240 19 10476920 intergenic variant C/T snv 0.37 14
rs763361
CD226
0.689 0.520 18 69864406 missense variant T/A;C snv 4.0E-06; 0.52 21
rs2542151 0.763 0.480 18 12779948 upstream gene variant G/T snv 0.83 11
rs7234029
PTPN2
0.807 0.320 18 12877061 intron variant A/G snv 0.27 7
rs16939895
PTPN2
1.000 0.120 18 12821904 intron variant G/A snv 0.17 1
rs12232497 0.701 0.360 17 39883866 intergenic variant T/C snv 0.35 18
rs3743930
MEFV
0.611 0.720 16 3254626 missense variant C/G;T snv 7.1E-02 43
rs12598357 0.724 0.240 16 28329624 intergenic variant A/G snv 0.43 15
rs12928404
ATXN2L
0.724 0.240 16 28835925 splice region variant T/C snv 0.44 0.45 15
rs117372389
NKD1
0.724 0.240 16 50634166 3 prime UTR variant G/T snv 1.1E-02 14
rs77150043
ADCY7
0.724 0.240 16 50270338 intron variant C/T snv 0.17 14
rs11466018
MEFV
0.827 0.200 16 3254739 missense variant A/G snv 6.6E-03 2.2E-03 7
rs12708716
CLEC16A
0.807 0.320 16 11086016 intron variant A/G snv 0.37 7
rs6498169
CLEC16A
0.807 0.280 16 11155472 non coding transcript exon variant G/A snv 0.66 6
rs12917716
CLEC16A
0.851 0.200 16 11095291 intron variant G/C snv 0.51 4